Abstract
Polymyxins are used as last-resort antibiotics, where other treatments have been ineffectual due to antibiotic resistance. However, resistance to polymyxins has also been now reported, therefore it is instructive to characterise at the molecular level, the mechanisms of action of polymyxins. Here we review insights into these mechanisms from molecular dynamics simulations and discuss the utility of simulations as a complementary technique to experimental methodologies.
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Introduction
Polymyxins are often used as last-resort antibiotics in cases in which others have failed. In particular they are used to treat infections caused by the Gram-negative ‘superbugs’: Acinetobacter baumannii, Pseudomonas aeruginosa and Klebsiella pneumoniae. (Velkov et al. 2016; Zavascki et al. 2007; Evans et al. 1999) Here we review mechanistic findings of polymyxin B1 (PMB1) and polymyxin E (colistin) permeation across the cell envelope of Gram-negative bacteria from computational studies; we note that this is not an exhaustive review but serves to highlight some key findings from simulation studies.
Polymyxins are a class of lipopeptide antibiotics produced by Paenibacillus polymyxa, as a defence mechanism against Gram-negative bacteria found in soil. (Benedict and Langlykke 1947) The general structure of polymyxins is a heptapeptide loop, a tripeptide side chain and a fatty acid chain (Fig. 1A). Five α,γ-diaminobutyric acid (Dab) residues confer an overall charge of +5 e. PMB1 and colistin are the most commonly used polymyxins in the clinic, their structures differ by a single residue (D-Phe/D-Leu respectively)(Velkov et al. 2010; Storm et al. 1977), and they are thought to share similar mechanisms of action. (Kwa et al. 2007) The most widely accepted theory of polymyxin movement across the outer membrane is that this occurs via a ‘self-promoted uptake’(Hancock 1984; Hancock 1997; Zhang et al. 2000; Hancock and Bell 1988) mechanism, while theories of cell lysis by polymyxins include barrel-stave insertion(Hancock 1997; Shai 1999; Dupuy et al. 2018; Khondker and Rheinstädter 2020), carpet insertion(Shai 1999; Khondker and Rheinstädter 2020; Deris et al. 2014) and polymyxin-mediated phospholipid (PL) exchange between the outer and inner membranes. (Clausell et al. 2007; Cajal et al. 1996) Insights into the mode of action of polymyxins have generally come from experimental studies, but in recent years, computational methods such as molecular dynamics (MD) simulations have become increasingly utilised to probe polymyxin behaviour. The recent increase in the number of MD studies of polymyxins has been enabled by the development of detailed atomistic and coarse grained (CG) models of the outer membrane (Lee et al. 2019; Hsu et al. 2017; Hsu et al. 2016). MD simulations provide details at the atomistic or near-atomistic level of resolution (Fig. 1B), albeit with the caveat that the simulated timescales are relatively short (μs).
Polymyxin interactions with the outer membrane
The outer membrane of Gram-negative bacteria contains lipopolysaccharide (LPS) in the outer leaflet and a mixture of PLs in the inner leaflet. The precise composition of both leaflets varies depending on the bacterial species. (Sohlenkamp and Geiger 2016; Di Lorenzo et al. 2021) LPS is a complex glycolipid consisting of a lipid A moiety (with 4–6 acyl tails) attached to an oligosaccharide core, which may be attached to a highly variable O-antigen polysaccharide (Fig. 1C). LPS molecules are non-covalently cross-linked by divalent cations (Ca2+ or Mg2+). The sugar regions of LPS present an energetic barrier to hydrophobic molecules, while the lipid A tails present a barrier to polar molecules. (Carpenter et al. 2016)
It is thought that polymyxins move across the outer membrane via the ‘self-promoted uptake’ mechanism, first proposed by Hancock et al. (Hancock 1984; Hancock 1997; Zhang et al. 2000; Hancock and Bell 1988). The first step in the mechanism is binding of the polymyxin cationic moieties to the anionic groups of LPS, with concomitant displacement of divalent cations that cross-link LPS molecules. (Teuber and Bader 1976; Wiese et al. 1998) The sequence of events following this is unclear but is thought to involve destabilisation of the outer membrane structure, thereby easing subsequent uptake of polymyxins. This destabilisation may take the form of transient ‘openings’ in the outer membrane(Hancock 1997; Hancock and Bell 1988) through which other molecules can pass, or it may be linked to increased fluidity of the outer membrane. (Hancock 1997) Experimental studies(Deris et al. 2014; Salazar et al. 2017; Ryder et al. 2014; Halder et al. 2015), particularly recent biophysical investigations of assembled outer membrane models(Dupuy et al. 2018; Han et al. 2018; Paracini et al. 2018; Oh et al. 2017), allow the study of polymyxin-outer membrane interactions, but atomistic level resolution cannot be readily achieved.
Data from molecular simulations supports the initial stages of the proposed ‘self-promoted uptake’ mechanism while providing additional details on subsequent stages. Based on this, the movement of polymyxins through the outer membrane of polymyxin-susceptible bacterial strains may involve the following stages:
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1.
Interaction with LPS sugar residues(Berglund et al. 2015; Jefferies et al. 2017; Fu et al. 2020; Ongwae et al. 2020; Feigman et al. 2018; Santos et al. 2017; Jiang et al. 2021a)
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2.
Polymyxin binding to lipid A headgroups(Berglund et al. 2015; Jefferies et al. 2017; Fu et al. 2020; Ongwae et al. 2020; Feigman et al. 2018; Santos et al. 2017; Jiang et al. 2021a; Li et al. 1862; Jiang et al. 2020a; b; Li et al. 2020; Jiang et al. 2021b)
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3.
Polymyxin insertion (insertion of polymyxin hydrophobic moieties into hydrophobic membrane core)(Berglund et al. 2015; Jefferies et al. 2017; Fu et al. 2020; Ongwae et al. 2020; Li et al. 1862; Jiang et al. 2020a; b; Li et al. 2020; Jiang et al. 2021b)
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4.
Polymyxin translocation (movement of the full polymyxin molecules into and through the hydrophobic membrane core)(Jefferies et al. 2017; Jiang et al. 2020a; b; Jiang et al. 2021b).
Interaction of polymyxin with LPS
Polymyxins form long-lived, electrostatic interactions with the saccharide moieties
In atomistic (we use all atom and united atom under the umbrella term ‘atomistic’) and coarse-grained simulations, polymyxins have been shown to directly interact with ReLPS (lipid A + Kdo) sugars, forming interactions with Kdo carboxyl groups via their Dab residues(Berglund et al. 2015; Jefferies et al. 2017; Santos et al. 2017) and with inner core heptose phosphates in membranes with more complete LPS models. (Ongwae et al. 2020; Feigman et al. 2018) Atomistic simulations of the interaction between PMB1 and outer membrane models show that PMB1 Dab residues are able to cross-link LPS Kdo sugars, with each PMB1 forming an average of ~8 hydrogen bonds with LPS. (Berglund et al. 2015) PMB1s bind to the LPS sugars for ~1.8 μs, preventing PMB1s from reaching the lipid A headgroups during the 2.2 μs simulation. The longevity of such interactions is also reported from other MD simulations(Jefferies et al. 2017; Ongwae et al. 2020) and indicates that the LPS sugars may act as a kinetic barrier to polymyxins permeating to the LPS headgroups. In 3-5 μs unbiased CG simulations of PMB1s interacting with an asymmetric RaLPS:PL bilayer (PMB1/LPS ratios of 1:4, 1:2, 1:1), PMB1s are mostly found to not penetrate deeper than the heptose sugars of RaLPS. (Jiang et al. 2021a) As part of this study, a one dimensional free energy profile generated for the movement of a single PMB1 from the 1:1 LPS: PL bilayer indicates that while the free energy initially decreases on moving through the LPS sugar region, it rapidly increases on moving into the Kdo sugar region. (Jiang et al. 2021a)
Extensive aggregation on LPS saccharides occurs in some simulation studies
Interestingly in some atomistic and coarse-grained simulations of ReLPS-containing systems, PMB1 aggregation on the membrane is observed, (Berglund et al. 2015; Fu et al. 2020) while in other comparable simulations, extensive aggregation is not observed. (Jefferies et al. 2017; Santos et al. 2017) This may be due to the lower polymyxin/LPS ratios (5:100(Jefferies et al. 2017), 6:100 (Santos et al. 2017) used in the latter simulations compared to those used in simulations in which aggregation was observed (38:100(Berglund et al. 2015), (9:100, 12:100, 15:100) (Fu et al. 2020)). These ratios are worked out simply by using the total number of polymyxin and LPS molecules reported for each simulation system. It should be noted that the number of water molecules, and therefore PMB1 concentrations, in each simulation study is not always reported; thus, quantitative comparisons regarding concentrations are not possible. This is further complicated by the issue of conversion between different levels of resolution.
Counterions play an important role in determining polymyxin-LPS interactions
Jefferies et al. perform CG simulations of PMB1 interacting with a symmetric ReLPS bilayer neutralised with either Ca2+ or Na+ ions. (Jefferies et al. 2017) In these simulations, it takes less time for PMB1 to permeate through the ReLPS sugars to reach the Lipid A headgroups when Na+ ions are present compared to Ca2+. Furthermore, PMB1 is able to penetrate slightly deeper into the outer membrane in the presence of Na+.
Polymyxin binding to lipid A headgroups
Having negotiated the layers of sugars, PMB1 next encounters the lipid A headgroups which are cross-linked by divalent counterions (Mg2+, Ca2+). In agreement with structure-activity relationship data(Velkov et al. 2010), simulations show that PMB1 binding to lipid A headgroups involves electrostatic interactions between the cationic PMB1 Dab residues and the anionic lipid A phosphate groups (Fig. 2) (Berglund et al. 2015; Jefferies et al. 2017; Fu et al. 2020; Ongwae et al. 2020; Feigman et al. 2018; Santos et al. 2017; Li et al. 1862; Jiang et al. 2020a; Jiang et al. 2020b; Li et al. 2020) Counterion displacement upon PMB1 binding was proposed as a key step of the original ‘self-promoted uptake’ mechanism. (Hancock 1984; Hancock 1997; Zhang et al. 2000; Hancock and Bell 1988) The strongest evidence of this from MD is provided by measurement of Ca2+ ion diffusion rates before and after polymyxin binding from atomistic simulations of PMB1 binding to a variety of lipid A/ReLPS bilayers. (Santos et al. 2017) In this study, Ca2+ ion lateral diffusion coefficients increase by at least 2-fold following PMB1 binding, with the increase being larger for lipid A bilayers compared to ReLPS bilayers. Fu et al. report similar observations in their CG simulations with the Ca2+ dissociation rate increasing with increasing PMB1 concentration. (Fu et al. 2020)
Free energy changes upon polymyxin binding
Jefferies et al. report potential-of-mean-force (PMF) free energy profiles of PMB1 moving from bulk solution to a ReLPS bilayer from CG simulations. (Jefferies et al. 2017) The results indicate that as polymyxins move through the ReLPS sugars towards the lipid A phosphate groups, the free energy decreases due to the favourable enthalpic contributions, despite the entropy change being unfavourable. The unfavourable entropy change is attributed to membrane ordering, specifically phosphate crystallisation induced by PMB1 binding, rather than decrease in conformational entropy of PMB1. Interestingly atomistic PMF profiles generated by Jiang et al. show favourable enthalpy change of polymyxin-lipid A binding, −17 to −13 kJ/mol. (Jiang et al. 2020a, b) The differences in simulation resolution, length and protocols makes direct, quantitative comparison of these studies difficult.
Polymyxin insertion into outer membrane core
Difficulties in sampling polymyxin insertion
In both simulations and experiment, polymyxins are found to insert their hydrophobic residues and/or acyl tails into the hydrophobic membrane core after binding to the lipid A headgroups (Fig. 2). (Han et al. 2018; Paracini et al. 2018) In unbiased atomistic and coarse-grained simulations, it is difficult to sample insertion events due to the slow diffusion of LPS. (Berglund et al. 2015; Jefferies et al. 2017; Fu et al. 2020) Replacing Ca2+ ions with Na+ ions(Berglund et al. 2015; Jefferies et al. 2017), reducing LPS to just lipid A molecules(Berglund et al. 2015; Santos et al. 2017; Li et al. 1862; Jiang et al. 2020a, b; Jiang et al. 2021b; Santos et al. 2017) and using symmetric bilayers (the latter strategy provides two leaflets of LPS; therefore, simulation time is not ‘wasted’ by PMBs interacting with PLs)(Berglund et al. 2015; Jefferies et al. 2017; Fu et al. 2020; Ongwae et al. 2020; Santos et al. 2017; Li et al. 1862) are common strategies used to bypass this difficulty. These strategies have been used to observe (mostly) isolated insertion events in a select few simulations into lipid A bilayers (atomistic)(Berglund et al. 2015; Li et al. 2020), ReLPS (CG) bilayers(Jefferies et al. 2017; Fu et al. 2020) and in one case into a full atomistic LPS bilayer(Ongwae et al. 2020). Polymyxin insertion is also seen in simulations employing enhanced simulations such as umbrella sampling to calculate free energies. (Jefferies et al. 2017; Jiang et al. 2020a, b; Jiang et al. 2021b) PMF profiles from these simulations (both atomistic and CG) predict that polymyxin translocation towards the hydrophobic membrane core is accompanied by an increase in free energy.
Folded amphipathic structure may be important for translocation
Interestingly in two studies in which atomistic steered-MD and umbrella sampling are employed,(Jiang et al. 2020a, b) following insertion, polymyxins adopt a folded amphipathic structure during translocation, which enables them to simultaneously maintain interactions with lipid A phosphates (via their Dab residues) and with lipid A acyl tails (via their hydrophobic moieties). This structure is in agreement with a model of PMB1 interacting with lipid A derived from NMR data. (Mares et al. 2009) Furthermore, in a very recent combined in silico and in vitro study, enhanced sampling simulations are used to observe the translocation of a peptide (PMB3), which has similar bactericidal activities to the polymyxins but differs structurally by the absence of a chiral methyl group on the acyl tail, with alanine substitutions at various positions. (Jiang et al. 2021b) This study highlights the role of specific residues in translocation and provides a good example of correlation of in silico data with experimental measures of OM disorganisation and MICs (in vitro) in A. baumannii. (Jiang et al. 2021b)
Polymyxin permeation towards the inner leaflet of the outer membrane
Following binding and insertion into the core of the outer membrane, the next steps are movement through the inner leaflet to enter the periplasm. (Hancock and Bell 1988) Jiang et al. report the molecular details of membrane disruption on polymyxin translocation. Their simulations show that polymyxin translocation is accompanied by 3-4 bound lipid A molecules being pulled into the membrane core. (Jiang et al. 2020a, b) This creates a pore-like structure in the membrane through which water and ions can permeate. Subsequently equilibrium simulations were initiated from a snapshot of one of the umbrella sampling windows in which the pore was present. Additional colistin molecules were added to the water on the lipid A side of the membrane. The pore persisted throughout the simulation and one colistin molecule spontaneously entered it from solution. (Jiang et al. 2020a)
Notably, when colistin is pulled past the centre of the membrane, towards the PLs of the inner leaflet, the pore closes in the final windows of umbrella sampling simulations, with lipid A molecules returning to the outer leaflet. (Jiang et al. 2020b) To our knowledge, this is to date the only example of late-stage ‘self-promoted uptake’ observed in an MD simulation, in which the membrane damage induced by polymyxin aids the uptake of another polymyxin. Biophysical data on the interaction of PMB1 with an asymmetric PL-LPS bilayer shows that partial polymyxin translocation occurs, with perturbation of membrane structural properties (reduction of membrane thickness, mixing of lipids between leaflets). (Paracini et al. 2018) Other experimental data shows conclusively that the outer membrane is not lethally damaged by polymyxin permeation; thus, the persistence of pores in simulations is likely a result of short simulation timescales and the slow-moving nature of LPS. (Sabnis et al. 2021; MacNair et al. 2018)
We note here that a number of simulation studies exist in which the interaction of polymyxins with modified LPS-containing membranes are reported: these are beyond the scope of this short review. (Salazar et al. 2017; Santos et al. 2017; Li et al. 1862; Jiang et al. 2020b; Li et al. 2020)
Dynamics of polymyxins in the periplasm
Having permeated across the outer membrane, polymyxins next encounter the aqueous periplasm. This cell envelope compartment is densely crowded with proteins and osmolytes and also contains the cell wall (peptidoglycan). To our knowledge at the time of writing this review, there is only one published simulation study of polymyxins in the periplasm. Pedebos et al report atomistic simulations of PMB1 in a range of periplasm models crowded to differing extents, from very dilute to realistic crowded volume fractions (Fig. 3A). (Pedebos et al. 2021) Long-lived associations between PMB1 and various periplasmic proteins and the cell wall are reported. From a mechanistic perspective, the most interesting finding is the spontaneous binding of PMB1 (via its acyl tail) to the lipoprotein carriers LolA (Fig. 3C) and LolB (Fig. 3B). It is hypothesised that LolA carrying polymyxins across the periplasm may be one mechanism via which these antibiotics reach the inner membrane. While currently there is no direct evidence to either support or disprove this simulation-generated hypothesis, it should be noted that transcriptomics data for E. coli does show increased LolA transcription on PMB1 treatment, providing some indirect support. (Tao et al. 2012)
Dynamics of polymyxins in the inner membrane
Cell lysis occurs as a result of polymyxin action on the inner membrane. Some insights into this action have been gleaned from MD simulations. In atomistic simulations of PMB1 molecules interacting with a symmetric bilayer composed of a mixture of PLs, Berglund et al. find polymyxins initially from hydrogen bonds with PLs via their Dab residues before spontaneously inserting their acyl tails into the membrane core within 100 ns of binding to the membrane (Fig. 2). (Berglund et al. 2015) This is followed by translocation towards the inner leaflet, in which polymyxins adopt the folded amphipathic conformation seen in other experimental(Mares et al. 2009) and simulation studies(Jiang et al. 2020a, c), accompanied by extensive membrane disruption. (Berglund et al. 2015) No aggregation is reported in these simulations, with polymyxins translocating as monomers, bearing similarities to the barrel-stave model of peptide insertion. (Shai 1999; Khondker and Rheinstädter 2020) In coarse-grained simulations of PMB1 interacting with a compositionally simpler inner membrane model at varying polymyxin/PL ratios, Fu et al. observe similar polymyxin binding and insertion behaviour with the degree of insertion depending on polymyxin/PL ratio. (Fu et al. 2020) However, here polymyxin translocation and membrane disruption are not observed. Instead polymyxins aggregated on the membrane, and an increase in bilayer bending rigidity is reported(Fu et al. 2020). The observed increase in area per lipid and reduction in membrane thickness with increasing polymyxin/PL provides some support for the carpet model of peptide insertion. (Shai 1999; Khondker and Rheinstädter 2020) Thus, the two simulation studies show similarities but also some striking differences.
To determine the membrane physical properties affecting PMB1-PL membrane interactions, Khondker et al. perform atomistic simulations of mixed PL bilayers with varying ratios of the constituent lipids and polymyxin/PL ratios (2:100–10:100). Some simulations are initiated from configurations from X-ray data. (Khondker et al. 2019) While the lipids used are not representative of those found in Gram-negative bacteria, they are chosen to assess the impact of membrane surface charge (POPS (1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-L-serine)) and lipid acyl chain packing (DMPS (1,2-dimyristoyl-sn-glycero-3-phospho-L-serine)) on PMB1-PL interaction. (Khondker et al. 2019) Polymyxins are found to insert into membranes with POPS, with the extent of insertion increasing with POPS fraction and hence increasing surface charge, in a mechanism similar to that observed by Berglund et al. (Berglund et al. 2015) However, with DMPS-containing bilayers, polymyxins are found to lie flat on the surface of the membrane, with aggregation occurring more readily on DMPS-containing bilayers than POPS-containing bilayers. (Khondker et al. 2019) This mechanism of interaction has some similarities to that observed by Fu et al. (Fu et al. 2020) The authors use their data to define a mathematical model for predicting polymyxin insertion depth. (Khondker et al. 2019)
We note that A. baumannii can form an outer membrane without LPS, which is believed to confer polymyxin resistance to the bacterium. (Moffatt et al. 2010) The LPS-free outer membrane is effectively a PL bilayer, and hence simulation studies of its interactions with colistin merit discussion. In umbrella sampling simulations, Jiang et al. show that colistin binding to their LPS-deficient model outer membrane model is energetically unfavourable, due to the lower surface charge relative to LPS-containing bilayers(Jiang et al. 2020b) This is in broad agreement with recent work by Edwards and co-workers which has shown that polymyxins pass through the inner membrane by interacting with the small quantities of LPS present in it. (Sabnis et al. 2021; Humphrey et al. 2021) Zhu et al. also perform atomistic simulations of symmetric bilayers representing LPS-deficient A. baumannii membranes with varying proportions of PG lipids (lipids with phosphatidylglycerol headgroup). At PG concentrations >35:65 (PG: other lipids) colistin molecules are found to bind preferentially to the anionic PG lipids, leading to a reduction in lipid lateral diffusion. (Zhu et al. 2020) No insertion or translocation is reported, but this is likely due to the short timescales (100 ns) of the simulations. (Zhu et al. 2020) Both the Jiang and Zhu studies highlight the importance of PL charge in polymyxin-PL interactions, in agreement with the work of Khondker et al. (Khondker et al. 2019)
Fu et al. report CG simulations of the interaction of a vesicle and planar bilayer (both composed of a mixture of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine (POPG) and 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine (POPE)) in the presence/absence of a single PMB1. In both scenarios, the vesicle and bilayer contact and exchange lipids, but contact occurs faster in the presence of PMB1 (~18 ns vs ~260 ns), across 3 repeat simulations. PMB1 acts as a contact site between the vesicle and the planar bilayer by adopting a conformation in which the hydrophobic moieties of the antibiotic insert into the vesicle and bilayer. (Fu et al. 2020) This provides support to the theory that polymyxin-mediated PL exchange between inner and outer Gram-negative membranes may contribute to cell lysis. This theory originated from experimental work including studies which showed that PMB1, but not polymyxin B nonapeptide (PMB1 without the fatty acyl tail) is able to induce fast PL exchange in POPG(Clausell et al. 2007; Cajal et al. 1996; Clausell et al. 2006) and POPE/POPG(Grau-Campistany et al. 2016) vesicles. Interestingly, recent transcriptomics data shows upregulation of genes involved in the Mla system on polymyxin treatment, which is involved in maintaining PL levels in both membranes(Henry et al. 2015), providing some support for polymyxin-mediated PL exchange. (Mann et al. 2021)
Summary
In summary, MD simulations have provided mechanistic insights into the action of polymyxins on both the inner and outer membranes of Gram-negative bacteria. There has been less work reported on the dynamics of polymyxins in the periplasm, but early work suggests a complex series of interactions with native proteins and the cell wall. Thus, details of the dynamic behaviour of polymyxins within all three compartments of the cell envelopes of Gram-negative behaviour are now beginning to emerge. Nevertheless, we still do not have a comprehensively characterised molecular-level picture of the complete process of cell lysis as some questions remain about the individual steps involved: (i) how do polymyxin aggregates cross the outer membrane, given the outer membrane is not completely disrupted by polymyxin permeation? (ii) What is the precise mechanism of their action at the inner membrane? (Does it involve any interactions with native membrane proteins?) (iii) How do polymyxins cross the periplasm—as monomers, aggregates, via simple diffusion, via binding to lipoprotein carriers or a combination of all of these?
As we have shown, MD simulations are playing an increasingly significant role in addressing these questions. However, as with all scientific measurement/prediction methods, MD simulations have their own set of limitations and caveats. The most impactful of these for mechanistic studies of biological systems is the relatively short time and length scales that are accessible. This is partly mitigated by CG models, in which the lower resolution is compensated by longer timescales and larger simulation systems. (David et al. 2019) While the CG simulation studies of polymyxins reported in the literature to date have employed the Martini set of CG force fields, encouragingly a number of other CG force fields now exist which are also well suited for the simulation of biological membrane systems. (Orsi and Essex 2011; Machado et al. 2019) The MARTINI force field has the advantages of having a wide library of parameterised lipids including LPS already available and allowing automated system setup for flat membrane, vesicles, nanodiscs and micelles via the CharmmGui webserver. (Hsu et al. 2017) The latest version of the force field, MARTINI3, has an expanded repertoire of particle types, but some bacterial lipids remain to be parametrised. (Souza et al. 2021) One slight caveat with the MARTINI force fields is that the secondary structure of proteins is fixed, so conformational changes in proteins are not accessible (other than inter-domain motions). In this context, this is only a slight caveat as such conformational changes are likely not of particular importance to the mechanistic studies of polymyxins. However, this issue is addressed by the SIRAH(Machado et al. 2019) force field in which secondary structure of proteins is not fixed.
Ultimately, it is desirable to go beyond a mechanistic understanding of polymyxins such that computational methods can be employed to inform the design of novel, more potent antibiotics, particularly as resistance to polymyxins has now emerged. (Binsker et al. 2021; Jeannot et al. 2017) To achieve this, calculations that provide quantitative comparisons of, e.g. free energies of membrane permeation of de novo designed candidate antibiotics are required. Currently, such comparisons are particularly problematic for studies of the outer membrane due to the slow-moving nature of LPS. (Shearer et al. 2020) Thus, methodological advancements are needed to enable more efficient convergence of free energy calculations using, for example, metadynamics and umbrella sampling such that high-throughput comparative computational studies can be performed. (Armacost et al. 2020) The intense research efforts into improved computational methodologies combined with ever-increasing availability of high-performance computing resources are highly likely to soon deliver the capabilities for simulation-informed de novo antibiotic design.
References
Armacost KA, Riniker S, Cournia Z (2020) Novel directions in free energy methods and applications. Journal of Chemical Information and Modeling 60(1):1–5. https://doi.org/10.1021/acs.jcim.0c01266
Benedict RG, Langlykke AF (1947) Antibiotic activity of Bacillus polymyxa. J Bacteriol 54(1):24
Berglund NA, Piggot TJ, Jefferies D, Sessions RB, Bond PJ, Khalid S (2015) Interaction of the antimicrobial peptide polymyxin B1 with both membranes of E. coli: a molecular dynamics study. PLOS Computational Biology 11(4):e1004180. https://doi.org/10.1371/journal.pcbi.1004180
Binsker U, Käsbohrer A, Hammerl JA (2021) Global colistin use: a review of the emergence of resistant Enterobacterales and the impact on their genetic. FEMS Microbiol Rev 1–37. https://doi.org/10.1093/femsre/fuab049
Cajal Y, Rogers J, Berg OG, Jain MK (1996) Intermembrane molecular contacts by polymyxin B mediate exchange of phospholipids. Biochemistry 35(1):299–308. https://doi.org/10.1021/bi9512408
Carpenter TS, Parkin J, Khalid S (2016) The free energy of small solute permeation through the Escherichia coli outer membrane has a distinctly asymmetric profile. J Phys Chem Lett 7(17):3446–3451. https://doi.org/10.1021/acs.jpclett.6b01399
Clausell A, Rabanal F, Garcia-Subirats M, Asunción Alsina M, Cajal Y (2006) Membrane association and contact formation by a synthetic analogue of polymyxin B and its fluorescent derivatives. The Journal of Physical Chemistry B 110(9):4465–4471. https://doi.org/10.1021/jp0551972
Clausell A, Garcia-Subirats M, Pujol M, Busquets MA, Rabanal F, Cajal Y (2007) Gram-negative outer and inner membrane models: insertion of cyclic cationic lipopeptides. The Journal of Physical Chemistry B 111(3):551–563. https://doi.org/10.1021/jp064757+
David JS, Jeffery BK, Alexander JS (2019) Simulation best practices for lipid membranes [Article v1.0]. Living J Comput Mol Sci 1(1):5966. https://doi.org/10.33011/livecoms.1.1.5966
Deris ZZ, Swarbrick JD, Roberts KD, Azad MA, Akter J, Horne AS, Nation RL, Rogers KL, Thompson PE, Velkov T, Li J (2014) Probing the penetration of antimicrobial polymyxin lipopeptides into gram-negative bacteria. Bioconjug Chem 25(4):750–760. https://doi.org/10.1021/bc500094d
Di Lorenzo F, Duda KA, Lanzetta R, Silipo A, De Castro C, Molinaro A (2021) A journey from structure to function of bacterial lipopolysaccharides. Chem Rev. https://doi.org/10.1021/acs.chemrev.0c01321
Dupuy FG, Pagano I, Andenoro K, Peralta MF, Elhady Y, Heinrich F, Tristram-Nagle S (2018) Selective interaction of colistin with lipid model membranes. Biophysical Journal 114(4):919–928. https://doi.org/10.1016/j.bpj.2017.12.027
Evans ME, Feola DJ, Rapp RP (1999) Polymyxin B sulfate and colistin: old antibiotics for emerging multiresistant gram-negative bacteria. Ann Pharmacother 33(9):960–967. https://doi.org/10.1345/aph.18426
Feigman MS, Kim S, Pidgeon SE, Yu Y, Ongwae GM, Patel DS, Regen S, Im W, Pires MM (2018) Synthetic Immunotherapeutics against Gram-negative pathogens. Cell Chem Biol 25(10):1185-1194.e5. https://doi.org/10.1016/j.chembiol.2018.05.019
Fu L, Wan M, Zhang S, Gao L, Fang W (2020) Polymyxin B loosens lipopolysaccharide bilayer but stiffens phospholipid bilayer. Biophysical Journal 118(1):138–150. https://doi.org/10.1016/j.bpj.2019.11.008
Grau-Campistany A, Manresa Á, Pujol M, Rabanal F, Cajal Y (2016) Tryptophan-containing lipopeptide antibiotics derived from polymyxin B with activity against Gram positive and Gram negative bacteria. Biochim Biophys Acta 1858(2):333–343. https://doi.org/10.1016/j.bbamem.2015.11.011
Halder S, Yadav KK, Sarkar R, Mukherjee S, Saha P, Haldar S, Karmakar S, Sen T (2015) Alteration of Zeta potential and membrane permeability in bacteria: a study with cationic agents. Springerplus 4:672. https://doi.org/10.1186/s40064-015-1476-7
Han ML, Velkov T, Zhu Y, Roberts KD, Le Brun AP, Chow SH, Gutu AD, Moskowitz SM, Shen HH, Li J (2018) Polymyxin-induced lipid A deacylation in Pseudomonas aeruginosa perturbs polymyxin penetration and confers high-level resistance. ACS Chem Biol 13(1):121–130. https://doi.org/10.1021/acschembio.7b00836
Hancock REW (1984) Alterations in outer membrane permeability. Annual Review of Microbiology 38(1):237–264. https://doi.org/10.1146/annurev.mi.38.100184.001321
Hancock RE (1997) Peptide antibiotics. Lancet 349(9049):418–422. https://doi.org/10.1016/S0140-6736(97)80051-7
Hancock RE, A Bell (1988) Antibiotic uptake into gram-negative bacteria. Journal of Clinical Microbiology and Infectious Diseases 7(6):713–720. https://doi.org/10.1007/BF01975036
Henry R, Crane B, Powell D, Deveson Lucas D, Li Z, Aranda J, Harrison P, Nation RL, Adler B, Harper M, Boyce JD, Li J (2015) The transcriptomic response of Acinetobacter baumannii to colistin and doripenem alone and in combination in an in vitro pharmacokinetics/pharmacodynamics model. J Antimicrob Chemother 70(5):1303–1313. https://doi.org/10.1093/jac/dku536
Hsu P-C, Jefferies D, Khalid S (2016) Molecular dynamics simulations predict the pathways via which pristine fullerenes penetrate bacterial membranes. The Journal of Physical Chemistry B 120(43):11170–11179. https://doi.org/10.1021/acs.jpcb.6b06615
Hsu P-C, Bruininks BMH, Jefferies D, Cesar Telles de Souza P, Lee J, Patel DS, Marrink SJ, Qi Y, Khalid S, Im W (2017) CHARMM-GUI Martini Maker for modeling and simulation of complex bacterial membranes with lipopolysaccharides. Journal of Computational Chemistry 38(27):2354–2363. https://doi.org/10.1002/jcc.24895
Humphrey M, Larrouy-Maumus GJ, Furniss RCD, Mavridou DAI, Sabnis A, Edwards AM (2021) Colistin resistance in Escherichia coli confers protection of the cytoplasmic but not outer membrane from the polymyxin antibiotic. Microbiology 167(11). https://doi.org/10.1099/mic.0.001104
Jeannot K, Bolard A, Plésiat P (2017) Resistance to polymyxins in Gram-negative organisms. Int J Antimicrob Agents 49(5):526–535. https://doi.org/10.1016/j.ijantimicag.2016.11.029
Jefferies D, Hsu PC, Khalid S (2017) Through the lipopolysaccharide glass: a potent antimicrobial peptide induces phase changes in membranes. Biochemistry 56(11):1672–1679. https://doi.org/10.1021/acs.biochem.6b01063
Jiang X, Yang K, Yuan B, Han M, Zhu Y, Roberts KD, Patil NA, Li J, Gong B, Hancock REW, Velkov T, Schreiber F, Wang L, Li J (2020) Molecular dynamics simulations informed by membrane lipidomics reveal the structure–interaction relationship of polymyxins with the lipid A-based outer membrane of Acinetobacter baumannii. Journal of Antimicrobial Chemotherapy 75(12):3534–3543. https://doi.org/10.1093/jac/dkaa376
Jiang X, Yang K, Han M-L, Yuan B, Li J, Gong B, Velkov T, Schreiber F, Wang L, Li J (2020) Outer membranes of polymyxin-resistant acinetobacter baumannii with phosphoethanolamine-modified lipid A and lipopolysaccharide loss display different atomic-scale interactions with polymyxins. ACS Infectious Diseases 6(10):2698–2708. https://doi.org/10.1021/acsinfecdis.0c00330
Jiang X, Yang K, Yuan B, Gong B, Wan L, Patil NA, Swarbrick JD, Roberts KD, Schreiber F, Wang L, Velkov T, Li J (2020) Simulations of octapeptin–outer membrane interactions reveal conformational flexibility is linked to antimicrobial potency. Journal of Biological Chemistry 295(47):15902–15912. https://doi.org/10.1074/jbc.RA120.014856
Jiang X, Sun Y, Yang K, Yuan B, Velkov T, Wang L, Li J (2021) Coarse-grained simulations uncover Gram-negative bacterial defense against polymyxins by the outer membrane. Computational and Structural Biotechnology Journal 19:3885–3891. https://doi.org/10.1016/j.csbj.2021.06.051
Jiang X, Patil NA, Azad MAK, Wickremasinghe H, Yu H, Zhao J, Zhang X, Li M, Gong B, Wan L, Ma W, Thompson PE, Yang K, Yuan B, Schreiber F, Wang L, Velkov T, Roberts KD, Li J (2021) A novel chemical biology and computational approach to expedite the discovery of new-generation polymyxins against life-threatening Acinetobacter baumannii. Chemical Science 12(36):12211–12220. https://doi.org/10.1039/D1SC03460J
Khondker A, Rheinstädter MC (2020) How do bacterial membranes resist polymyxin antibiotics? Communications Biology 3(1):77. https://doi.org/10.1038/s42003-020-0803-x
Khondker A, Dhaliwal AK, Saem S, Mahmood A, Fradin C, Moran-Mirabal J, Rheinstädter MC (2019) Membrane charge and lipid packing determine polymyxin-induced membrane damage. Communications Biology 2(1):67. https://doi.org/10.1038/s42003-019-0297-6
Kwa A, Kasiakou SK, Tam VH, Falagas ME (2007) Polymyxin B: similarities to and differences from colistin (polymyxin E). Expert Rev Anti Infect Ther 5(5):811–821. https://doi.org/10.1586/14787210.5.5.811
Lee J, Patel DS, Ståhle J, Park SJ, Kern NR, Kim S, Lee J, Cheng X, Valvano MA, Holst O, Knirel YA, Qi Y, Jo S, Klauda JB, Widmalm G, Im W (2019) CHARMM-GUI membrane builder for complex biological membrane simulations with glycolipids and lipoglycans. J Chem Theory Comput 15(1):775–786. https://doi.org/10.1021/acs.jctc.8b01066
Li J, Beuerman R, Verma CS (1862) Mechanism of polyamine induced colistin resistance through electrostatic networks on bacterial outer membranes. Biochim Biophys Acta Biomembr 2020(9):183297. https://doi.org/10.1016/j.bbamem.2020.183297
Li J, Beuerman R, Verma CS (2020) Dissecting the molecular mechanism of colistin resistance in mcr-1 bacteria. J Chem Inf Model 60(10):4975–4984. https://doi.org/10.1021/acs.jcim.0c01051
Machado MR, Barrera EE, Klein F, Sóñora M, Silva S, Pantano S (2019) The SIRAH 2.0 Force Field: Altius, Fortius, Citius. Journal of Chemical Theory and Computation 15(4):2719–2733. https://doi.org/10.1021/acs.jctc.9b00006
MacNair CR, Stokes JM, Carfrae LA, Fiebig-Comyn AA, Coombes BK, Mulvey MR, Brown ED (2018) Overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics. Nat Commun 9(1):458. https://doi.org/10.1038/s41467-018-02875-z
Mann D, Fan J, Somboon K, Farrell DP, Muenks A, Tzokov SB, DiMaio F, Khalid S, Miller SI, Bergeron JRC (2021) Structure and lipid dynamics in the maintenance of lipid asymmetry inner membrane complex of A. baumannii. Communications Biology 1(4):817. https://doi.org/10.1038/s42003-021-02318-4
Mares J, Kumaran S, Gobbo M, Zerbe O (2009) Interactions of lipopolysaccharide and polymyxin studied by NMR spectroscopy. J Biol Chem 284(17):11498–11506. https://doi.org/10.1074/jbc.M806587200
Moffatt JH, Harper M, Harrison P, Hale JD, Vinogradov E, Seemann T, Henry R, Crane B, St Michael F, Cox AD, Adler B, Nation RL, Li J, Boyce JD (2010) Colistin resistance in Acinetobacter baumannii is mediated by complete loss of lipopolysaccharide production. Antimicrob Agents Chemother 54(12):4971–4977. https://doi.org/10.1128/AAC.00834-10
Oh YJ, Plochberger B, Rechberger M, Hinterdorfer P (2017) Characterizing the effect of polymyxin B antibiotics to lipopolysaccharide on Escherichia coli surface using atomic force microscopy. J Mol Recognit 30(6). https://doi.org/10.1002/jmr.2605
Ongwae GM, Morrison KR, Allen RA, Kim S, Im W, Wuest WM, Pires MM (2020) Broadening activity of polymyxin by quaternary ammonium grafting. ACS Infectious Diseases 6(6):1427–1435. https://doi.org/10.1021/acsinfecdis.0c00037
Orsi M, Essex JW (2011) The ELBA force field for coarse-grain modeling of lipid membranes. PLOS ONE 6(12):e28637. https://doi.org/10.1371/journal.pone.0028637
Paracini N, Clifton LA, Skoda MWA, Lakey JH (2018) Liquid crystalline bacterial outer membranes are critical for antibiotic susceptibility. Proceedings of the National Academy of Sciences 115(32) https://doi.org/10.1073/pnas.1803975115
Pedebos C, Smith I, Boags A, Khalid S (2021) The hitchhiker’s guide to the periplasm: Unexpected molecular interactions of polymyxin B1 in E.coli. 29(5)444–456. https://doi.org/10.1016/j.str.2021.01.009
Ryder MP, Wu X, McKelvey GR, McGuire J, Schilke KF (2014) Binding interactions of bacterial lipopolysaccharide and the cationic amphiphilic peptides polymyxin B and WLBU2. Colloids Surf B Biointerfaces 120:81–87. https://doi.org/10.1016/j.colsurfb.2014.05.004
Sabnis A, Hagart KLH, Klöckner A, Becce M, Evans LE, Furniss RCD, Mavridou DAI, Murphy R, Stevens MM, Davies JC, Larrouy-Maumus GJ, Clarke TB, Edwards AM (2021) Colistin kills bacteria by targeting lipopolysaccharide in the cytoplasmic membrane. eLife 10:e65836. https://doi.org/10.7554/eLife.65836
Salazar J, Alarcón M, Huerta J, Navarro B, Aguayo D (2017) Phosphoethanolamine addition to the Heptose I of the Lipopolysaccharide modifies the inner core structure and has an impact on the binding of Polymyxin B to the Escherichia coli outer membrane. Archives of Biochemistry and Biophysics 620:28–34. https://doi.org/10.1016/j.abb.2017.03.008
Santos DES, Pol-Fachin L, Lins RD, Soares TA (2017) Polymyxin binding to the bacterial outer membrane reveals cation displacement and increasing membrane curvature in susceptible but not in resistant lipopolysaccharide chemotypes. J Chem Inf Model 57(9):2181–2193. https://doi.org/10.1021/acs.jcim.7b00271
Shai Y (1999) Mechanism of the binding, insertion and destabilization of phospholipid bilayer membranes by α-helical antimicrobial and cell non-selective membrane-lytic peptides. Biochimica et Biophysica Acta (BBA) - Biomembranes 1462(1):55–70. https://doi.org/10.1016/S0005-2736(99)00200-X
Shearer J, Marzinek JK, Bond PJ, Khalid S (2020) Molecular dynamics simulations of bacterial outer membrane lipid extraction: adequate sampling? The Journal of Chemical Physics 153(4):044122. https://doi.org/10.1063/5.0017734
Sohlenkamp C, Geiger O (2016) Bacterial membrane lipids: diversity in structures and pathways. FEMS Microbiology Reviews 40(1):133–159. https://doi.org/10.1093/femsre/fuv008
Souza PCT, Alessandri R, Barnoud J, Thallmair S, Faustino I, Grünewald F, Patmanidis I, Abdizadeh H, Bruininks BMH, Wassenaar TA, Kroon PC, Melcr J, Nieto V, Corradi V, Khan HM, Domański J, Javanainen M, Martinez-Seara H, Reuter N, Best RB, Vattulainen I, Monticelli L, Periole X, Tieleman DP, de Vries AH, Marrink SJ (2021) Martini 3: a general purpose force field for coarse-grained molecular dynamics. Nat Methods 18(4):382–388. https://doi.org/10.1038/s41592-021-01098-3
Storm DR, Rosenthal KS, Swanson PE (1977) Polymyxin and related peptide antibiotics. Annu Rev Biochem 46:723–763. https://doi.org/10.1146/annurev.bi.46.070177.003451
Tao K, Narita S-I, Tokuda H (2012) Defective lipoprotein sorting induces lolA expression through the Rcs stress response phosphorelay system. Journal of bacteriology 194(14):3643–3650. https://doi.org/10.1128/JB.00553-12
Teuber M, Bader J (1976) Action of polymyxin B on bacterial membranes. Archives of Microbiology 109(1):51–58. https://doi.org/10.1007/BF00425112
Velkov T, Thompson PE, Nation RL, Li J (2010) Structure--activity relationships of polymyxin antibiotics. J Med Chem 53(5):1898–1916. https://doi.org/10.1021/jm900999h
Velkov T, Roberts KD, Thompson PE, Li J (2016) Polymyxins: a new hope in combating Gram-negative superbugs? Future Med Chem 8(10):1017–1025. https://doi.org/10.4155/fmc-2016-0091
Wiese A, Münstermann M, Gutsmann T, Lindner B, Kawahara K, Zähringer U, Seydel U (1998) Molecular mechanisms of polymyxin B-membrane interactions: direct correlation between surface charge density and self-promoted transport. J Membr Biol 162(2):127–138. https://doi.org/10.1007/s002329900350
Zavascki AP, Goldani LZ, Li J, Nation RL (2007) Polymyxin B for the treatment of multidrug-resistant pathogens: a critical review. J Antimicrob Chemother 60(6):1206–1215. https://doi.org/10.1093/jac/dkm357
Zhang L, Dhillon P, Yan H, Farmer S, Hancock RE (2000) Interactions of bacterial cationic peptide antibiotics with outer and cytoplasmic membranes of Pseudomonas aeruginosa. Antimicrob Agents Chemother 44(12):3317–3321. https://doi.org/10.1128/aac.44.12.3317-3321.2000
Zhu Y, Lu J, Han M-L, Jiang X, Azad MAK, Patil NA, Lin Y-W, Zhao J, Hu Y, Yu HH, Chen K, Boyce JD, Dunstan RA, Lithgow T, Barlow CK, Li W, Schneider-Futschik EK, Wang J, Gong B, Sommer B, Creek DJ, Fu J, Wang L, Schreiber F, Velkov T, Li J (2020) Polymyxins bind to the cell surface of unculturable Acinetobacter baumannii and cause unique dependent resistance. Advanced Science 7(15):2000704. https://doi.org/10.1002/advs.202000704
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Weerakoon, D., Petrov, K., Pedebos, C. et al. Polymyxin B1 within the E. coli cell envelope: insights from molecular dynamics simulations. Biophys Rev 13, 1061–1070 (2021). https://doi.org/10.1007/s12551-021-00869-8
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DOI: https://doi.org/10.1007/s12551-021-00869-8